| Tag | Content |
|---|
EnhancerAtlas ID | HS044-02484 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr11:61872350-61873810 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr11:61873527-61873542 | TTTTATTTTTAGTAC | - | 6.09 | | SRF | MA0083.3 | chr11:61872758-61872774 | TTACCCTATATGGTCT | + | 6.07 | | STAT1 | MA0137.3 | chr11:61872815-61872826 | TTTCCTGGAAA | - | 6.62 | | Stat4 | MA0518.1 | chr11:61872812-61872826 | CCTTTTCCTGGAAA | - | 6.91 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I062104 | chr11 | 61871666 | 61874160 |
|
Enhancer Sequence | CAAAAACCAC CAGCAACAAC AACAACAAAA CACCTCTTTC CTTTATATAA GTTACCCAGT 60
CTCAGGTATT TCTTCATAGC AGTGTGGGAA TGAACTAATA CAGGTGACTA CTCACATGTG 120
GCAAATGCAG ACAAGGGCAC TCTGTGCTAT TGGGATGCTG AGGTGGGGGT GTGATAGGAG 180
TTTGGCAGGA CTTGTTTCCC AAGACATAGG TCACAAGGAC CCCCCTGATA AAACAGGATG 240
TGGTAAAGGA GCCAGCCAAA ACCCCCCAAA ACCAAGATGG TGATGAAAGC GACCCTTGGT 300
CCTCTCACCG CTCATTATAC ACTAATCATA ATCCATGATT TGTCCATGGT GAAGGAAACT 360
CCCACCAGAA ACACGACAGC TTACATACGC CATGGCAACA TCCGGAAGTT ACCCTATATG 420
GTCTAAAAAG GGGAGGAACT CTCATTTCTG GGAATTCTCT GACCTTTTCC TGGAAAATTC 480
ATGAATAAGC CACCCTTGTT TAGCATGTGA GCAAGAAACA AACATAAAAA TAGCAACCTG 540
CAACTCTCAC GGCTGCTCTT CCGATGGCAT AGCCACTCTT ACTCCTTTAC TTTTAAAATA 600
AACTTGCTTT CACTTTACTC TGTTAACTCT TGAATTCCTT CCTGTGCAAA GCCAAGAACT 660
CACGTCGCCT CCTGGGCTGA ACTCCAATGT GGGGGTTCAC CCTGTGACAG GTGGATGGGC 720
TGGAGTCCAG GAGTTCGGGT CCAGCCTAAG CAACATAGTG AGACCCCCCA TCTCTATTTT 780
TTTCTCAGAC AGTATAAGAG ACAGATGAAG CAAAGTGCAT AAATGGCTGT GAGGAGCATG 840
TGGTTTGTCA AAGCTGGAAC TTTATTTACA AACAAGTTCC AGCATTATCT GAGTGGGTGC 900
TGCTAACAAT TATAGCGTGT TCTTTCAAAC TGCAGACTGG GATTAGACGG TTTGCCAAAA 960
AGCCACTGAG TACATCAAAG CGAGAATTCT GAATTCTCCA TTTATCTTCA GATTTATCAC 1020
TCCCTCCCTC TGTGCCCTTC TCTGCATCTG CTGTATGTGA GTATGGAGAG TCCACACAAT 1080
TCAGTCTGTA CCAGTGGTCT AGGTTTTCAA CTACATCTCA TTGGTCAAGC ATGTTTGCAT 1140
TCACAGAAGG AACCCTACCC CCATTTTTGT TTTCCTGTTT TATTTTTAGT ACATTTTAGG 1200
CCTTAAGAAT GTAGGGTTTT TTTGTTTGTT TTTTTTTCCT ATGAGACGGG AGTCTTGCTC 1260
CATAACCCAG GCTGGAATGC AGTGGCATGA TCTCGGCTCA CTGCAACCTC CCCGTCCCGG 1320
GTTCAAGCGA TTCTCCTGCC TCAGCCTCCC ATGTAGCTAG GAATACAGGC ATGCACCACC 1380
ATGCCTGGCT AATTTTTTTT TTAATTTTTT TTTTAATTTT TAGTAGAGAC GGGGTTTCAC 1440
CATGTTGGCC AGACTTGTTT 1460
|
